ASPIRATOR VENTURI SYSTEM MODEL 55-JV
K-Number: K813319 · 1981-12-14
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Device Summary
Frequently Asked Questions
What is the ASPIRATOR VENTURI SYSTEM MODEL 55-JV?
ASPIRATOR VENTURI SYSTEM MODEL 55-JV is a medical device that received FDA 510(k) clearance on 1981-12-14. The listed applicant is J. H. Emerson Co.. The 510(k) number is K813319.
When did ASPIRATOR VENTURI SYSTEM MODEL 55-JV receive FDA 510(k) clearance?
ASPIRATOR VENTURI SYSTEM MODEL 55-JV received FDA 510(k) clearance on 1981-12-14, under 510(k) number K813319.
Who is the listed applicant for ASPIRATOR VENTURI SYSTEM MODEL 55-JV?
The FDA 510(k) record lists J. H. Emerson Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASPIRATOR VENTURI SYSTEM MODEL 55-JV?
The FDA product code for ASPIRATOR VENTURI SYSTEM MODEL 55-JV is GCX.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing J. H. Emerson Co. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: GCX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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